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Recruiting Phase 2 Interventional

A Study of TAK-411 in Adults With Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)

ClinicalTrials.gov ID: NCT06798012

Public ClinicalTrials.gov record NCT06798012. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 17, 2026, 2:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Open-label, Proof-of-Concept Study to Investigate the Efficacy, Safety, and Tolerability of TAK-411 in Adult Subjects With Chronic Inflammatory Demyelinating Polyradiculoneuropathy (The CASCA Study)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

CIDP is an autoimmune disease. This means that the body's germ fighting (immune) system attacks itself. In CIDP, the immune system attacks the protective covering around the nerves called myelin. Over time, these nerves lose their ability to send signals to the muscles in the body. This leads to muscle weakness and loss of sensation in arms and legs among other symptoms. Participants with CIDP can be treated with a protein called immunoglobulin (or IG). TAK-411 is a special type of immune globulin G (hsIgG) that has been chemically changed. It is made from IG that comes from human plasma. This study will test if TAK-411 can decrease inflammation and improve symptoms of CIDP. The main aim of this study is to check how TAK-411 affects the physical functioning of adults with CIDP when compared with results of the placebo group of a historical trial. Participants may be treated with TAK-411 for up to 1 year (51 weeks) and will be followed up for 3 weeks after last dose. During the study, participants may visit their study clinic up to approximately 21 times.

Study identification

NCT ID
NCT06798012
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
36 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 13, 2025
Primary completion
Dec 1, 2027
Completion
Jun 7, 2028
Last update posted
Apr 22, 2026

2025 – 2028

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
University of California San Diego La Jolla California 92093 Recruiting
California Pacific Medical Center San Francisco California 94109 Recruiting
UF Health Neurology - Jacksonville Jacksonville Florida 32209 Recruiting
Visionary Investigators Network Miami Florida 33133 Recruiting
University of South Florida Tampa Florida 33612 Recruiting
Emory University Atlanta Georgia 30322 Recruiting
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 Recruiting
Mayo Clinic Rochester Rochester Minnesota 55905 Recruiting
The Curators of the University of Missouri on behalf of University of Missouri Health Care Columbia Missouri 65212-0001 Recruiting
The Washington University St Louis Missouri 63110 Recruiting
Penn Blood Disorders Program - Hospital of The University of Pennsylvania Philadelphia Pennsylvania 19104 Recruiting
Houston Methodist Research Institute Houston Texas 77030 Not yet recruiting
University of Washington Seattle Washington 98195 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06798012, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 22, 2026 · Synced Sep 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06798012 live on ClinicalTrials.gov.

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